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Merck
CN

333638

4-Propoxybenzaldehyde

97%

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About This Item

Linear Formula:
CH3CH2CH2OC6H4CHO
CAS Number:
5736-85-6
Molecular Weight:
164.20
UNSPSC Code:
12352100
PubChem Substance ID:
24860159
MDL number:
MFCD00014134

Key Documents

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Product Name

4-Propoxybenzaldehyde, 97%

InChI

1S/C10H12O2/c1-2-7-12-10-5-3-9(8-11)4-6-10/h3-6,8H,2,7H2,1H3

SMILES string

CCCOc1ccc(C=O)cc1

InChI key

FGXZWMCBNMMYPL-UHFFFAOYSA-N

assay

97%

form

liquid

refractive index

n20/D 1.546 (lit.)

bp

129-130 °C/10 mmHg (lit.)

density

1.039 g/mL at 25 °C (lit.)

functional group

aldehyde

Application

4-Propoxybenzaldehyde was used in the preparation of (2S,4S,5R)-(±)-2-(4-propoxyphenyl)-3,4-dimethyl-5-phenyl-1,3-oxazolidine via condensation with 1-ephedrine.

General description

Kinetic constants for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-propoxybenzaldehyde was evaluated.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR8222
MKCC3322
MKCB9271
MKBW2084V
MKBP4711V

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C-HO and CH (arene) interactions in (2S, 4S, 5R)-(-)-2-(4-propoxyphenyl)-3, 4-dimethyl-5-phenyl-1, 3-oxazolidine.
Duffy M, et al.
AZo Journal of Materials Online, 60(2), o234-o236 (2004)
Dalila Rocco et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-12)
The preparation of 24-functionalized 12,22:26,32-terpyridines (4'-functionalized 3,2:6',3''-terpyridines) by the reaction of three 4-alkoxybenzaldehydes with 3-acetylpyridine and ammonia was investigated; under identical reaction conditions, two (R = nC4H9, C2H5) gave the expected products whereas a third (R = nC3H7) gave only
M Jiménez et al.
Journal of agricultural and food chemistry, 49(8), 4060-4063 (2001-08-22)
A kinetic study of the inhibition of mushroom tyrosinase by 4-substituted benzaldehydes showed that these compounds behave as classical competitive inhibitors, inhibiting the oxidation of L-3,4-dihydroxyphenylalanine (L-DOPA) by mushroom tyrosinase (o-diphenolase activity). The kinetic parameter (K(I)) characterizing this inhibition was

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